Literature DB >> 19425590

Cobalt-catalyzed arylzincation of alkynes.

Kei Murakami1, Hideki Yorimitsu, Koichiro Oshima.   

Abstract

Cobalt(II) bromide catalyzes arylzincation of alkynes with arylzinc iodide x lithium chloride complexes in acetonitrile. The scope of the arylzincation is wide enough to use unfunctionalized alkynes, such as 6-dodecyne, as well as arylacetylenes. The inherent functional group compatibility of arylzinc reagents allows preparation of various functionalized styrene derivatives. The reaction is applicable to the efficient and stereoselective synthesis of a synthetic estrogen and its derivative.

Entities:  

Year:  2009        PMID: 19425590     DOI: 10.1021/ol900883j

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Nickel-catalyzed reductive arylation of activated alkynes with aryl iodides.

Authors:  Stephanie C M Dorn; Andrew K Olsen; Rachel E Kelemen; Ruja Shrestha; Daniel J Weix
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

2.  Divergent ring-opening coupling between cyclopropanols and alkynes under cobalt catalysis.

Authors:  Junfeng Yang; Yixiao Shen; Yang Jie Lim; Naohiko Yoshikai
Journal:  Chem Sci       Date:  2018-07-16       Impact factor: 9.825

3.  Recent advances in transition-metal-catalyzed intermolecular carbomagnesiation and carbozincation.

Authors:  Kei Murakami; Hideki Yorimitsu
Journal:  Beilstein J Org Chem       Date:  2013-02-11       Impact factor: 2.883

  3 in total

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